Details for TG:c.2610G>T, p.Glu870His

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
133900662132888417
VARIANT EFFECT None
ANNOTATION FLAG None
GENE TG
REFERENCE ALLELE G
ALTERNATE ALLELE T
TRANSCRIPT N.A.
CDNA CHANGE c.2610G>T
PROTEIN CHANGE p.Glu870His
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00180.00080.00140.00.0030.0041

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.0030580.00079980.0025779.948e-050.00.0022690.0043580.0031010.003337

ESP
AAEA
0.00045390.004186
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousPossibly Damaging2.976916Polymorphism
DBSNP ID NA
1 combination linked to TG:c.2610G>T, p.Glu870His OLI1026
1 disease linked to TG:c.2610G>T, p.Glu870His Congenital hypothyroidism
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